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Background and Aim Obesity affects the gut microbiome, which in turn increases the risk for colorectal cancer. Several studies have shown the mechanisms by which some bacteria may influence the development of colorectal cancer; however, gut microbiome characteristics in obese patients with colorectal cancer remain unclear. Therefore, this study evaluated their gut microbiome profile and its relationship with metabolic markers. Methods The study assessed fecal samples from 36 consecutive patients with colorectal cancer and 38 controls without colorectal cancer. To identify microbiotic variations between patients with colorectal cancer and controls, as well as between nonobese and obese individuals, 16S rRNA gene amplicon sequencing was performed. Results Principal coordinate analysis showed significant differences in the overall structure of the microbiome among the study groups. The α‐diversity, assessed by the Chao1 index or Shannon index, was higher in patients with colorectal cancer versus controls. The relative abundance of the genera Enterococcus, Capnocytophaga, and Polaribacter was significantly altered in obese patients with colorectal cancer, whose serum low‐density lipoprotein concentrations were positively correlated with the abundance of the genus Enterococcus; among the most abundant species was Enterococcus faecalis, observed at lower levels in obese versus nonobese patients. Conclusions This study demonstrated several compositional alterations of the gut microbiome in patients with colorectal cancer and showed that a reduced presence of E. faecalis may be associated with obesity‐related colorectal cancer development. The gut microbiome may provide novel insights into the potential mechanisms in obesity‐related colorectal carcinogenesis., This study demonstrated that a reduced presence of Enterococcus faecalis may be associated with the obesity‐related colorectal cancer development. The gut microbiome may provide novel insights for the potential mechanisms in obesity‐related colorectal carcinogenesis.

We previously found that surprisingly many V2 neurons showed selective responses to particular angles embedded within continuous contours [M. Ito & H. Komatsu (2004)Journal of Neuroscience, 24, 3313-3324]. Here, we addressed whether the selectivity is dependent on the presence of individual constituent components or on the unique combination of these components. To reveal roles of constituent half-lines in response to whole angles, we conducted a quantitative model study after the framework of cascade models. Our linear-non-linear summation model implemented a few subunits selective to particular half-lines and was fitted to neuronal responses for each neuron. The study indicates that the best-fitting models well replicate the selectivity in the majority of V2 neurons and that the angle selectivity is dependent on a linear combination of responses to individual half-line components of the angles. The implication is that optimal angles are given by a combination of two preferred half-line components and the selectivity is sharpened by introducing suppression to non-preferred half-line components, rather than a specific facilitatory interaction between two preferred half-line components. The study indicates the participation of the gain control of responsiveness according to the number of half-line components. We also showed that the selectivity to acute angles depends on a combination of responses to one preferred component and weak responses to another component. Therefore, we concluded that the angle selectivity is dependent on selective responses to individual half-line components of the angles rather than a unique combination between them, whereas neurons could be selective to various angle widths at area V2.

Previous electrophysiological, neuroimaging and lesion studies have suggested that the anterior part of the monkey inferior temporal (IT) cortex, or area TE, plays an important role in colour processing. However, little is known about how colour information is distributed in these cortical regions. Here, we explored the distribution of colour-selective activity in alert macaque monkeys using functional magnetic resonance imaging (fMRI) with two types of stimuli: a multicoloured ('Mondrian') pattern and an isoluminant colour grating. These two types of stimuli are both commonly used in human fMRI studies, but Mondrian stimuli, which contain a richer variety of hues and hence might be more suitable for activating higher-order areas than grating stimuli, have not been used to examine colour-selectivity in higher-order areas in earlier monkey studies. With the Mondrian stimuli, we observed that areas along the ventral pathway, V1, V2/V3, V4 and the IT cortex, responded more strongly to colour stimuli than to luminance stimuli. In the IT cortex, we found that colour-selective activities are not distributed uniformly, but are localized in discrete regions, each extending several millimetres in the anterior or posterior part of the IT cortex. The colour-selective activation in the anterior IT was observed only with the Mondrian stimuli, whereas the colour-selective activation in the posterior IT was observed with both the Mondrian and grating stimuli, with little overlap. These findings suggest that there are multiple subregions with differing stimulus selectivities distributed in the IT cortex, and that colour information is processed in these discrete subregions.

Angles and junctions embedded within contours are important features to represent the shape of objects. To study the neuronal basis to extract these features, we conducted extracellular recordings while two macaque monkeys performed a fixation task. Angle stimuli were the combination of two straight half-lines larger than the size of the classical receptive fields (CRFs). Each line was drawn from the center to outside the CRFs in 1 of 12 directions, so that the stimuli passed through the CRFs and formed angles at the center of the CRFs. Of 114 neurons recorded from the superficial layer of area V2, 91 neurons showed selective responses to these angle stimuli. Of these, 41 neurons (36.0%) showed selective responses to wide angles between 60 degrees and 150 degrees that were distinct from responses to straight lines or sharp angles (30 degrees ). Responses were highly selective to a particular angle in approximately one-fourth of neurons. When we tested the selectivity of the same neurons to individual half-lines, the preferred direction was more or less consistent with one or two components of the optimal angle stimuli. These results suggest that the selectivity of the neurons depends on both the combination of two components and the responses to individual components. Angle-selective V2 neurons are unlikely to be specific angle detectors, because the magnitude of their responses to the optimal angle was indistinguishable from that to the optimal half-lines. We suggest that the extraction of information of angles embedded within contour stimuli may start in area V2.

Cells in adult primary visual cortex are capable of integrating information over much larger portions of the visual field than was originally thought. Moreover, their receptive field properties can be altered by the context within which local features are presented and by changes in visual experience. The substrate for both spatial integration and cortical plasticity is likely to be found in a plexus of long-range horizontal connections, formed by cortical pyramidal cells, which link cells within each cortical area over distances of 6-8 mm. The relationship between horizontal connections and cortical functional architecture suggests a role in visual segmentation and spatial integration. The distribution of lateral interactions within striate cortex was visualized with optical recording, and their functional consequences were explored by using comparable stimuli in human psychophysical experiments and in recordings from alert monkeys. They may represent the substrate for perceptual phenomena such as illusory contours, surface fill-in, and contour saliency. The dynamic nature of receptive field properties and cortical architecture has been seen over time scales ranging from seconds to months. One can induce a remapping of the topography of visual cortex by making focal binocular retinal lesions. Shorter-term plasticity of cortical receptive fields was observed following brief periods of visual stimulation. The mechanisms involved entailed, for the short-term changes, altering the effectiveness of existing cortical connections, and for the long-term changes, sprouting of axon collaterals and synaptogenesis. The mutability of cortical function implies a continual process of calibration and normalization of the perception of visual attributes that is dependent on sensory experience throughout adulthood and might further represent the mechanism of perceptual learning.

Experimental autoimmune myocarditis (EAM)-induced heart failure in rats is used to study the pathogenesis of heart failure. Based on a proteomic analysis of soluble (S) and membranous (M) fractions extracted from ventricles of rats with a stable chronic form of EAM-induced heart failure, we assessed changes in protein levels and their correlation to heart functions to gain insights into the pathogenesis and to explore new targets for the treatment of heart failure. Proteins were separated by two-dimensional gel electrophoresis and silver stained spots were analyzed. In the S-fraction, 274+/-3 spots were detected in the normal (N)-group and 273+/-6 in the heart failure (HF)-group. In the HF-group, 26 of the spots were increased and 15 were decreased in intensity. In the M-fraction, 277+/-3 spots were detected in the N-group and 277+/-2 in the HF-group, with 20 spots increased and 10 decreased in intensity. We analyzed relationships between the expression of these proteins and 11 parameters of heart function, and found all the significantly changed spots to correlate with at least one of the parameters. We analyzed 49 spots that correlated with over 9 parameters of heart function using mass spectrometry, and identified 15 as proteins with increased expression including glucose regulated protein (GRP)78, an endoplasmic-stress related protein, and heat shock protein (HSP)90beta, a molecular chaperone, and 4 spots as proteins with decreased expression. It is suggested that in the heart failure model, GRP78 and HSP90beta play a role in the protection or deterioration of the heart and may be new targets for treatment.

In order to study neuronal basis to extract Angles and junctions embedded within contours, we conducted extracellular recordings, while two macaque monkeys performed the fixation task. Angle stimuli were the combination of two straight half lines. Each line was drawn from the center to outside the classical receptive fields in one of 12 directions. In the superficial layer of area V2, 91 out of 114 neurons showed selective responses to these angle stimuli. Of these, 41 neurons (36%) showed selective responses to wide angles between 60° and 150°, which were distinct from responses to straight lines or sharp angles (30°). When we tested these neurons’ selectivity to the 12 individual half lines, the preferred directions were more or less consistent with one or two components of the optimal angle stimuli. These results suggest that the angle selectivity in area V2 was largely dependent on the representation of individual line components. We suggest that area V2 is the first step to extract information of angles embedded within contour stimuli.

In the early stages of the visual cortex (areas 17 and 18), it is well known that neurons respond to bar and contour stimuli. However, several recent studies reported that some neurons in this stage respond to uniform plane stimuli that cover the classical receptive fields [1, 2]. In order to better understand the neuronal mechanisms underlying surface representation in the early visual stages, we explored the distribution of activation to the uniform plane stimuli by using optical imaging of intrinsic signals and extracellular recordings from areas 17 and 18 of anesthetized cats. We also intended to examine the distribution of such activities in relation to the orientation preference map in the same areas.

Cells in the anterior part of the inferotemporal cortex (anterior IT) respond to moderately complex stimulus features of object images. To study dependency of their responses on contrast polarity of stimulus images, we selected cells with optimal stimuli that were defined only by shape and not related to texture or color, and examined effects of reversing the contrast of the image or removing it except for edges between dark and bright parts of the image ("outlining"). The contrast reversal produced a reduction of the response to the optimal stimulus by > 50% in 60% of tested cells; the outlining, in 70%. When the two transformations were considered together, 94% of the cells showed a reduction by > 50%. Effects of the transformations on shape selectivity were also studied by comparing responses to several different shapes each of whose contours were expressed in different ways. Statistically significant changes in relative effectiveness of the different shapes as a function of contour expression were observed in more than half of the cells. These results suggest that responses of individual cells in anterior IT carry information about contrast polarity as well as about shape.